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. Author manuscript; available in PMC: 2024 Dec 9.
Published in final edited form as: Cell Rep. 2019 Dec 10;29(11):3522–3538.e7. doi: 10.1016/j.celrep.2019.11.028

Table 1. SENP7-Interacting Proteins along with SUMOylation Site and Their Function in Disease.

Protein Name Condition of Identification SUMOylation Site SUMO Interaction Motif (SIM) Function Disease Reported
NCoR1a DSS 145/DAKK
repress NF-κB and AP-1 genes (Tiefenbach et al., 2006; Perissi et al., 2004) breast cancer
1068/IKQE
(Zhang et al., 2006)
1333IKFD

Notch1a DSS 1607/FKRD
1575-1579/VLVVL stem cell development, γδ T cell activation (Stier et al., 2002; Washburn et al., 1997) IBD, cancer
1712/VKSE
(Dahan et al., 2011)
2242/AKPE

CBX5a control/DSS 84/EKSE transcriptional activator breast cancer (Bawa-Khalfe et al., 2012)

PLK1a control/DSS 358/EKEE cell cycle (Wen et al., 2017) colorectal cancer (Takahashi et al., 2003)

Vimentina control/ DSS 373/MKEE epithelial-mesenchymal transition (Bawa-Khalfe et al., 2012) IBD (Andoh et al., 2002)

Birc2 control/ DSS 38/EKMK 424-428/IVSVL anti-apoptotic IBD (Grabinger et al., 2017)

40/MKFD 575-579/IVFIP

CARD9 DSS 165/LKEE 22-26/ISVID regulate gut microbiota IBD (Lamas et al., 2016)

219/MAKE
343-347/IEAIL
391/EKAD

S100A9 DSS 35/SKKE
calcium-binding protein IBD (Lee et al., 2012)
51/MKKE

E3 ubiquitin ligase SIAH2 control/DSS 250-254/VLLIG ubiquitination prostate cancer (Qi et al., 2013)
a

SUMOylation of these proteins is known.